Pages
Products

CP


Official Full Name
ceruloplasmin
Organism
Homo sapiens
Gene ID
1356
Background
The protein encoded by this gene is a metalloprotein that binds most of the copper in plasma and is involved in the peroxidation of Fe(II)transferrin to Fe(III) transferrin. Mutations in this gene cause aceruloplasminemia, which results in iron accumulation and tissue damage, and is associated with diabetes and neurologic abnormalities. Two transcript variants, one protein-coding and the other not protein-coding, have been found for this gene. [provided by RefSeq, Feb 2012]
Synonyms
CP-2; AB073614

Cat.No. Product Name Price
LV09607L human CP (NM_000096) lentivirus particles Inquiry
Cat.No. Product Name Price
SHH268465 shRNA set against Human CP (NM_003652.3) Inquiry
SHH268469 shRNA set against Mouse CP (NM_153107.2) Inquiry
SHH268473 shRNA set against Rat CP (NM_031766.1) Inquiry
SHW015200 shRNA set against Danio rerio CP (NM_131802) Inquiry
Cat.No. Product Name Price
MiUTR1M-03275 CP miRNA 3'UTR clone Inquiry
MiUTR1M-03276 CP miRNA 3'UTR clone Inquiry
MiUTR3H-00411 CP miRNA 3'UTR clone Inquiry
CDCB176675 Danio rerio CP ORF Clone (NM_131802) Inquiry
CDCB193440 Rabbit CP ORF clone (XM_008266309.1) Inquiry
CDCH383953 Human CP ORF clone(NM_000096.3) Inquiry
CDCR233656 Mouse Cp ORF Clone(NM_001042611.1) Inquiry
CDCR243701 Mouse Cp ORF Clone(NM_007752.2) Inquiry
CDCR377280 Rat Cp ORF Clone(NM_012532.2) Inquiry
Quick Inquiry